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NOT YET RECRUITING
NCT06051734

Early Detection of Cardiac Affection in Patients of Wilson's Disease

Sponsor: Assiut University

View on ClinicalTrials.gov

Summary

Wilson disease (WD) is a rare autosomal recessive disorder caused by a genetic defect in ATP7B resulting in limited excretion of excess copper into the bile Pathological copper accumulation occurs in the entire body, with the liver and the brain being primarily affected

Key Details

Gender

All

Age Range

Any - Any

Study Type

OBSERVATIONAL

Enrollment

50

Start Date

2023-10-01

Completion Date

2029-09-30

Last Updated

2023-09-25

Healthy Volunteers

No